VH Fillman - DNK 260947 - VikingHolstein

Production & Efficiency

Trait Index 80 100 120
Production 118
Milk kg 99
Fat, kg 110
Fat, % 110
Protein kg 117
Protein % 127
Persistency 104
Growth 94
Daily carcass gain 101
Carcass conformation score 90
Saved feed 95
Maintenance efficiency 103

NAV proof run date: 12-08-2025 Reliability 100 % Number of daughters: 8662

Expected Progeny Difference

Trait Index Bull effect Average
Milk kg, 305 days 99 -32.8 11600
Fat kg, 305 days 110 12.5 475
Fat %, 305 days 110 0.16 4.1
Protein kg, 305 days 117 17.0 406
Protein %, 305 days 127 0.20 3.5

NAV proof run date: 12-08-2025 Reliability 100 % Number of daughters: 8662

Health & Reproduction

Trait Index 80 100 120
Daughter fertility 113
Interval from calving to first insemination (cows) 98
Interval from first to last insemination (heifers) 121
Interval from first to last insemination (cows) 112
Number of inseminations (heifers) 117
Number of inseminations (cows) 111
Calving sire 100
Calving maternal 112
Udder health 107
General health 101
Longevity 109
Hoof health 98
Sole Ulcer 94
Sole Hemorrhage 105
Heel Horn Erosion 107
Digital dermatitis + Interdigital Dermatitis 100
Verrucose dermatitis + Interdigital Hyperplasia 97
Double sole + White line separation 105
Cork screw claw 105
Youngstock survival 99

NAV proof run date: 12-08-2025 Reliability 99 % Number of daughters: 7467

Functional

Trait Index 80 100 120
Milkability 86
Temperament 98

NAV proof run date: 12-08-2025 Reliability 97 % Number of daughters: 3351

Conformation

Trait Index 80 100 120
Frame 100
Stature 98 Short Tall
Body depth 86 Shallow Deep
Chest width 106 Narrow Wide
Rib structure 99 Coarse Angular
Top line 105 Weak Strong
Rump width 111 Narrow pins Wide pins
Rump angle 79 High pins Low pins
Feet & legs 97
Rear legs, side view 109 Straight Sickled
Rear legs, back rear view 97 Toes out Parallel, bow-legged
Foot angle 90 Low Steep
Bone quality 98 Coarse Fine and thin
Hock quality 103 Filled Dry
Udder 113
Fore udder attachment 104 Loose Strong
Rear udder height 107 Low High
Rear udder width 110 Narrow Wide
Udder support 100 Weak Strong
Udder depth 116 Deep High
Udder balance 94 Deep rear udder Deep front udder
Teat length 111 Short Long
Teat thickness 109 Thin Thick
Teat placement (front) 120 Wide Close
Teat placement (back) 107 Wide Close

NAV proof run date: 12-08-2025 Reliability 97 % Number of daughters: 3351

Monogenic

Name Scientific name Symptoms Code Result
BLAD Bovine Leukocyte Adhesion Deficiency (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal Read more (BLF = Not carrier, BLC = Single carrier, BLS = Double carrier) BLAD is an autosomal recessively inherited defect in the Holstein population. It is characterized by recurrent bacterial infections, delayed wound healing and stunted growth. Calves with BLAD are more susceptible to infections and their lifespan varies, many die shortly after birth. Osborndale Ivanhoe (US 1189870) has been identified as the key ancestor of the disorder. Several widely used sires after Osborndale, eg. Penstate Ivanhoe Star (US 1441440) and Carlin-M Ivanhoe Bell (US 1667366) are carriers of BLAD. https://omia.org/OMIA000595/9913/ BLF Free
HH1 Holstein Haplotype 1 (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal Read more (HH1F = Not carrier, HH1C = Single carrier, HH1S = Double carrier) HH1 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the North American Holstein population and primarily causes early embryonic death (spontaneous abortion), but abortion can occur throughout the gestation. The key ancestor is believed to be Pawnee Farm Arlinda Chief (US1427381). https://omia.org/OMIA000001/9913/ HH1F Free
HH3 Holstein Haplotype 3 (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal Read more (HH3F = Not carrier, HH3C = Single carrier, HH3S = Double carrier) HH3 is an autosomal recessively inherited defect in the Holstein population. The disorder has been identified in the North American and the Nordic Holstein population, however the frequency was somewhat lower in the Nordic population. HH3 primarily causes early embryonic death (spontaneous abortion), within the first 60 days of gestation. The key ancestors are believed to be Glendell Arlinda Chief (US 1556373) and Gray View Skyliner (US 1244845). https://omia.org/OMIA001824/9913/ HH3F Free
HH4 Holstein Haplotype 4 (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal Read more (HH4F = Not carrier, HH4C = Single carrier, HH4S = Double carrier) HH4 is an autosomal recessively inherited defect in the Holstein population. The disorder was identified in the French Holstein population and causes early embryonic death (spontaneous abortion). For animals that are a heterozygous for the gene, a reduction in fertility is seen. The effect is more pronounced in heifers than cows. The key ancestor is believed to be Besne Buck (FRA 4486041658). https://omia.org/OMIA001826/9913/ HH4F Free
RP1 Progressive retinal degeneration (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is Read more (RP1F = Not carrier, RP1C = Single carrier, RP1S = Double carrier) Progressive retinal degeneration is an autosomal recessively inherited defect. In the French Normande population, an association between homozygotic carrier animals of the RP1 gene and progressive blindness has been demonstrated. Blindness is due to a progressive degeneration of the photoreceptors. The RP1 mutation segregates within many cattle populations and is prevalent in e.g. the Finncattle population. For other breeds than Normande the phenotypic effect of the mutation is unclear. https://omia.org/OMIA000866/9913/ RP1F Free
HH6 Holstein Haplotype 6 (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal Read more (HH6F = Not carrier, HH6C = Single carrier, HH6S = Double carrier) HH6 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. The key ancestor is believed to be Gray View Skyliner (US 1244845). https://omia.org/OMIA002149/9913/ HH6F Free
HH7 Holstein Haplotype 7 (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal Read more (HH7F = Not carrier, HH7C = Single carrier, HH7S = Double carrier) HH7 is an autosomal recessively inherited defect in the Holstein population. It was identified in the French Holstein population and causes early embryonic death (spontaneous abortion), before 35 days of gestation. https://omia.org/OMIA001830/9913/ HH7F Free

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